人 SPG20 (NM_015087) cDNA克隆

Accession: NM_015087
基因名称: SPG20
基因别名: SPARTIN; TAHCCP1
基因描述: Homo sapiens spastic paraplegia 20 (Troyer syndrome) (SPG20), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2001 (查看编码区序列)
翻译后氨基酸长度: 666 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longest transcript. Variants 1, 2, 3, and 4 encode the same protein.
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G115744 人 SPG20 (NM_015087) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]